Introduction:
The course aims to provide participants with a comprehensive understanding of regulatory processes pertaining to risk management under the REACH and CLP Regulations. It will cover the entire process, from the initial steps taken by regulatory bodies to evaluate substances with specific claims, through Compliance Checks, Testing Proposals and Substance Evaluation, laying a solid foundation for understanding regulatory requirements. Additionally, participants will learn about the proper risk management measures adopted by regulatory bodies once a substance is deemed hazardous, such as inclusion in the SVHC list, Authorization list, Restrictions, and Harmonized Classification.
The course is therefore designed to equip participants with the necessary knowledge and skills, to navigate through the complex regulatory framework governing risk management under the REACH and CLP Regulations. It provides insights into the various members involved in different steps of the process and timelines related to each process.
Program:
- Evaluation Process under REACH
- Purpose
- Actors involved
- Assessment on Regulatory Needs
- Evaluation processes
- Testing proposals
- Compliance checks
- Substance evaluation
- Actions by registrants
- Regulatory Risk Management REACH
- Procedure for identifying an SVHC substance
- Proposal for Authorization and Annex XIV of REACH
- Restriction proposal and Annex XVII of REACH
- Regulatory Risk Management CLP
- Harmonized Classification Proposal and Annex VI of CLP
To whom:
This course is aimed at companies’ regulatory affairs, product safety and quality managers and to whom is willing to learn more about regulatory risk management procedures.
Teacher/Speaker:
Chiara Marelli
Language:
Italian
(available in English upon request)
Duration:
4 hours
Cost:
300 €/person
